815-23-6 Usage
Uses
Used in Pharmaceutical Synthesis:
Bromopentafluoroacetone is used as a key building block in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique reactivity and stability properties make it an essential component in the creation of complex molecular structures required for effective medicinal compounds.
Used in Agrochemical Production:
In the agrochemical industry, bromopentafluoroacetone is utilized as a fundamental component in the production of pesticides and other crop protection agents. Its role in the synthesis of these chemicals is crucial for enhancing agricultural productivity and ensuring food security by protecting crops from pests and diseases.
Used in High-Temperature and Acid-Resistant Applications:
Bromopentafluoroacetone is employed in industries that require materials capable of withstanding extreme conditions, such as high temperatures and exposure to strong acids. Its resistance to these harsh environments makes it suitable for applications in chemical processing, materials science, and other fields where durability and stability are paramount.
Used in Environmental and Health Monitoring:
Due to the potential toxicity and ozone depletion concerns associated with bromopentafluoroacetone and similar compounds, it is used as a subject of study in environmental and health monitoring programs. These initiatives aim to assess the impact of such chemicals on ecosystems and human health, guiding regulatory actions and informing the development of safer alternatives.
Check Digit Verification of cas no
The CAS Registry Mumber 815-23-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 815-23:
(5*8)+(4*1)+(3*5)+(2*2)+(1*3)=66
66 % 10 = 6
So 815-23-6 is a valid CAS Registry Number.
InChI:InChI=1/C3BrF5O/c4-2(5,6)1(10)3(7,8)9
815-23-6Relevant articles and documents
Interaction of perfluorinated α-fluorosulfatocarbonyl compounds with nucleophilic reagents
Delyagina, N. I.,Avetisyan, E. A.,Rogovik, V. M.,Cherstkov, V. F.,Sterlin, S. R.,German, L. S.
, p. 217 - 222 (1993)
α-Perfluorosulfatoperfluorocarbonyl compounds interact with alkaline metals halogenides to form the corresponding α-halo derivatives as a result of the direct nucleophilic substitution of the FSO3 group.Through the action of halogenide anions on perfluorinated α,β-bis-fluorosulfatocarbonyl compounds, substitution by halogen of the FSO3 group in the α-position to the carbonyl takes place.However, the FSO3 group in the β-position is cleaved, which allows α-substituted β-dicarbonyl derivatives to be obtained.
FLUOROALIPHATIC ESTERS OF FLUOROSULFONIC ACID. 4. REACTIONS OF α-FLUOROSULFATOPERFLUORO KETONES WITH NUCLEOPHILIC REAGENTS
Rogovik, V. M.,Delyagina, N. I.,Mysov, E. I.,Cherstov, V. F.,Sterlin, S. R.,German, L. S.
, p. 1879 - 1882 (2007/10/02)
α-Fluorosulfatoperfluoroethyl isopropyl ketone I and fluorosulfatopentafluoroacetone II react with alkali metal chlorides and bromides to form the corresponding α-haloperfluoro ketones as a result of direct nucleophilic substitution.
